| Identification | More | [Name]
4-Bromophenol | [CAS]
106-41-2 | [Synonyms]
4-BROMOHYDROXYBENZENE
4-BROMOPHENOL
4-Bromophenol p-Bromophenol
AKOS BBS-00004402
BROMOPHENOL-4
P-BROMOPHENOL
1,4-bromophenol
4-bromo-pheno
p-bromohydroxybenzene
p-bromophenicacid
p-bromo-pheno
Phenol, 4-bromo-
Phenol, p-bromo-
Phenol,4-bromo-
4-Bromophbenol
4-Bromophenoles
p-Bromophenoles
p-Bromophenol 4-Bromophenol
4-BROMOPHENOL, 1000MG, NEAT
Para Bromo Phenol | [EINECS(EC#)]
203-394-4 | [Molecular Formula]
C6H5BrO | [MDL Number]
MFCD00002313 | [Molecular Weight]
173.01 | [MOL File]
106-41-2.mol |
| Chemical Properties | Back Directory | [Appearance]
pinkish-brown crystalline solid | [Melting point ]
61-64 °C (lit.) | [Boiling point ]
235-236 °C (lit.) | [density ]
1.84 | [refractive index ]
1.5085 (estimate) | [Fp ]
235-238°C | [storage temp. ]
room temp | [solubility ]
14g/l | [form ]
Crystalline Solid | [pka]
9.37(at 25℃) | [color ]
Pinkish-brown | [Water Solubility ]
It is insoluble in water. It is soluble in 5%ethanol. | [Usage]
Intermediates of Liquid Crystals | [λmax]
282nm(EtOH)(lit.) | [Merck ]
14,1428 | [BRN ]
1680024 | [CAS DataBase Reference]
106-41-2(CAS DataBase Reference) | [NIST Chemistry Reference]
4-Bromophenol(106-41-2) | [Storage Precautions]
Store under inert gas;Light sensitive | [EPA Substance Registry System]
Phenol, 4-bromo- (106-41-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing . | [RIDADR ]
2811 | [WGK Germany ]
2
| [RTECS ]
SJ7960000
| [F ]
8-10-23 | [Hazard Note ]
Irritant | [TSCA ]
Yes | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29081900 | [Hazardous Substances Data]
106-41-2(Hazardous Substances Data) | [Toxicity]
mouse,LD50,intraperitoneal,411mg/kg (411mg/kg),Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 44(12), Pg. 19, 1979. |
| Hazard Information | Back Directory | [Chemical Properties]
4-Bromophenol is a pinkish-brown crystalline solid. four-sided biconical crystal precipitated from ether or chloroform. The melting point is 66.4 ℃, and a small amount of water can reduce the melting point a lot. Soluble in water, chloroform, easily soluble in ethanol, ether and glacial acetic acid, soluble in 7 parts of water. | [Uses]
4-Bromophenol is used as an intermediate in medicine grade. It is also used as a phenol that is used in Stille reactions. It is used in the intermediate of organic synthesis, flame retardant and pharmaceutical industry. | [Application]
4-Bromophenol is a phenolic derivative that It can used as a reagent in Stille reactions or Intermediates of Liquid Crystals. | [Definition]
ChEBI: 4-bromophenol is a bromophenol containing only hydroxy and bromo substituents that are para to one another. It has a role as a mouse metabolite, a persistent organic pollutant, a human xenobiotic metabolite, a rat metabolite, a human urinary metabolite and a marine metabolite. | [Preparation]
4-Bromophenol is synthesized by bromination of phenol. The bromine and carbon disulfide solution was added to the phenolic carbon disulfide solution, and the addition was started below 5°C, and the addition was completed under stirring for 2 hours. Phenol and bromine are approximately equimolar ingredients. Distill the reactant to remove carbon disulfide, and then conduct fractional distillation under reduced pressure to collect fractions at 145-150°C (3.32-3.99kPa) to obtain the product. Yield 80-84%. | [Synthesis Reference(s)]
Tetrahedron, 45, p. 7869, 1989 DOI: 10.1016/S0040-4020(01)85800-2
The Journal of Organic Chemistry, 23, p. 280, 1958 DOI: 10.1021/jo01096a033 | [Synthesis]
m-Bromoaniline (50 g) is dissolved by boiling in a mixture of water (400 ml) and sulfuric acid (50 ml). The solution is then cooled to 10℃ and diazotized by the addition of sodium nitrite (21 g) dissolved in a small amount of water, The resulting diazonium salt solution is run in a thin stream during fifteen to thirty minutes into a boiling mixture of water (300 ml) and sulfuric acid (100 ml) contained in a flask fitted with a dropping funnel, a steam inlet tube reaching to the bottom of the flask, and an efficient condenser set for downward distillation. During the addition of the diazonium salt solution the acid solution is heated so that its volume remains constant, and steam is passed in at such a rate that at the end of the addition approximately 1 liter of distillate has been collected. Steam distillation is then continued until 2-liters of distillate has been collected. To this is added sodium chloride (150 g), and the phenol is extracted with ether, using portions of 200, 100, and 100 ml. The ether is removed from the combined extracts and the product is distilled under reduced pressure. Eight runs of 50 g, each of m-bromoaniline gave 330 g of crude m-bromophenol boiling at 100-140℃ (20-30 mm.). Redistillation gave 313 g (77.8%) of m-bromophenol which boiled at 125-130℃ at 25 mm. Treatment of this 313 g of product with sodium hydroxide and methyl sulfate gave 285 g of m-bromoanisole (4-bromophenol), b. p. 100℃ at 20 mm[1].
| [Purification Methods]
Crystallise the phenol from CHCl3, CCl4, pet ether (b 40-60o), or water and dry it at 70o under vacuum for 2hours. [Beilstein 6 IV 1043.] | [References]
[1] Koelsch, C. Frederick. “The Preparation of m-Bromophenol.” Journal of the American Chemical Society 61 4 (1939): 969.
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